HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028816G>T , CM000667.2:g.135028816G>T | GRCh38 |
NC_000005.9:g.134364506G>T , CM000667.1:g.134364506G>T | GRCh37 |
NC_000005.8:g.134392405G>T | NCBI36 |
NG_012114.1:g.10459C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.908C>A MANE Select | ENSP00000265340.6:p.Pro303Gln | |
ENST00000265340.11:c.908C>A | ENSP00000265340.6:p.Pro303Gln | |
ENST00000506438.5:c.908C>A | ENSP00000427542.1:p.Pro303Gln | |
NM_002653.4:c.908C>A | NP_002644.4:p.Pro303Gln | |
NM_002653.5:c.908C>A MANE Select | NP_002644.4:p.Pro303Gln |